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1-(3-chloro-4-(trifluoromethyl)phenyl)-3-(4-nitrophenyl)urea is a complex organic compound with the molecular formula C14H8ClF3N4O3. It is a derivative of urea, featuring a 3-chloro-4-(trifluoromethyl)phenyl group attached to the nitrogen atom at position 1, and a 4-nitrophenyl group attached to the nitrogen atom at position 3. 1-(3-chloro-4-(trifluoromethyl)phenyl)-3-(4-nitrophenyl)urea is characterized by its unique structure, which includes a chlorine atom, a trifluoromethyl group, and a nitro group, all of which contribute to its chemical properties and potential applications. Due to its specific functional groups, it may be of interest in the fields of pharmaceuticals, agrochemicals, or as a precursor in the synthesis of other complex molecules. However, further research would be required to determine its specific uses and safety profile.

23745-41-7

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23745-41-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23745-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,4 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 23745-41:
(7*2)+(6*3)+(5*7)+(4*4)+(3*5)+(2*4)+(1*1)=107
107 % 10 = 7
So 23745-41-7 is a valid CAS Registry Number.

23745-41-7Relevant academic research and scientific papers

Design, synthesis and anticancer activities of diaryl urea derivatives bearing N-acylhydrazone moiety

Zhang, Bei,Zhao, Yanfang,Zhai, Xin,Wang, Lihui,Yang, Jingyu,Tan, Zehui,Gong, Ping

, p. 1046 - 1054 (2012/09/07)

A new series of diaryl urea derivatives bearing N-acylhydrazone moiety were designed and synthesized. All the target compounds were evaluated for their cytotoxic activities in vitro against human lung adenocarcinoma epithelial cell line (A549), human breast cancer cell line (MDA-MB-231) and human leukemia cell line (HL-60) by standard 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Several compounds (1a, 1f and 1h) were further evaluated against human embryonic fibroblast, lung-derived cell line (WI38). The pharmacological results indicated that some compounds exhibited promising anticancer activities. In particular, compound 1f showed the most potent cytotoxicity against the tested three cell lines with IC50 values of 0.41 μM, 0.24 μM and 0.23 μM, respectively.

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